Canonical Allele Identifier: CA379962129

Gene: WT1

Linked Data

• ClinVar Variation Id: 2151387
• ClinVar RCV Id: RCV003061316
• dbSNP Id: rs2133037185
• MyVariant Identifiers: chr11:g.32439160T>G (hg19) ; chr11:g.32417614T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32417614T>G , CM000673.2:g.32417614T>G	GRCh38
NC_000011.9:g.32439160T>G , CM000673.1:g.32439160T>G	GRCh37
NC_000011.8:g.32395736T>G	NCBI36
NG_009272.1:g.22928A>C , LRG_525:g.22928A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.928A>C	ENSP00000331327.5:p.Thr310Pro
ENST00000379077.9:c.928A>C	ENSP00000368368.5:p.Thr310Pro
ENST00000379079.8:c.277A>C	ENSP00000368370.2:p.Thr93Pro
ENST00000448076.9:c.928A>C	ENSP00000413452.5:p.Thr310Pro
ENST00000452863.10:c.928A>C MANE Select	ENSP00000415516.5:p.Thr310Pro
ENST00000639563.3:c.928A>C	ENSP00000492269.3:p.Thr310Pro
ENST00000640146.2:c.304A>C	ENSP00000491984.2:p.Thr102Pro
ENST00000332351.7:c.913A>C	ENSP00000331327.3:p.Thr305Pro
ENST00000379077.7:c.913A>C	ENSP00000368368.3:p.Thr305Pro
ENST00000379079.6:c.277A>C	ENSP00000368370.2:p.Thr93Pro
ENST00000448076.7:c.913A>C	ENSP00000413452.3:p.Thr305Pro
ENST00000452863.7:c.913A>C	ENSP00000415516.3:p.Thr305Pro
ENST00000527775.1:c.166A>C	ENSP00000435351.1:p.Thr56Pro
ENST00000530998.5:c.277A>C	ENSP00000435307.1:p.Thr93Pro
NM_000378.4:c.913A>C	NP_000369.3:p.Thr305Pro
NM_001198551.1:c.277A>C , LRG_525t2:c.277A>C	NP_001185480.1:p.Thr93Pro
NM_001198552.1:c.277A>C	NP_001185481.1:p.Thr93Pro
NM_024424.3:c.913A>C	NP_077742.2:p.Thr305Pro
NM_024426.4:c.913A>C	NP_077744.3:p.Thr305Pro
NM_000378.5:c.928A>C	NP_000369.4:p.Thr310Pro
NM_024424.4:c.928A>C	NP_077742.3:p.Thr310Pro
NM_024426.5:c.928A>C	NP_077744.4:p.Thr310Pro
NR_160306.1:n.1107A>C
NM_000378.6:c.928A>C	NP_000369.4:p.Thr310Pro
NM_001198552.2:c.277A>C	NP_001185481.1:p.Thr93Pro
NM_024424.5:c.928A>C	NP_077742.3:p.Thr310Pro
NM_024426.6:c.928A>C MANE Select	NP_077744.4:p.Thr310Pro